Diazyme 08896577190
Ref 08896577190
Diazyme 08896577190 is a kappa/lambda light chain immunoglobulin IVD (EU IVDR Class C) made by Diazyme Laboratories, Inc., registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 0817089021716XK) and listed in FDA GUDID since 21 Jul 2020 (UDI-DI 00817089023024), active as of 25 Oct 2026.
Active
CE IVDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR EUDAMED | Number0817089021716XK 00817089023024 | Date23 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00817089023024 | Date21 Jul 2020 | StatusListed |
Official records
- EUDAMED public site 0817089021716XK
- AccessGUDID record 00817089023024
Across registries
- EUDAMED Basic UDI-DI 0817089021716XK registered 23 Sep 2026 Active
- FDA GUDID UDI-DI 00817089023024 listed 21 Jul 2020 Listed
Timeline
- Listed FDA GUDID 00817089023024
- Registered EUDAMED 0817089021716XK
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Kappa-Lambda FLC Control Set EUDAMEDDiazyme GUDID
- Generic name
- Kappa/lambda light chain immunoglobulin IVD, control
- Device name
- Kappa/Lambda Free Light Chain Control Set
- Model / reference
- 08896577190
- Primary DI / UDI-DI
- 00817089023024
- Basic UDI-DI
- 0817089021716XK
- EMDN code
- W0102152003 Specific protein controls
- GMDN term
- Kappa/lambda light chain immunoglobulin IVD, control
- Device class
- Class C
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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